Canonical Allele Identifier: CA1602103043
Gene: NSG2 HGNC NCBI

Linked Data

dbSNP Id: rs911564033

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.174221073A>G , CM000667.2:g.174221073A>G GRCh38
NC_000005.9:g.173648076A>G , CM000667.1:g.173648076A>G GRCh37
NC_000005.8:g.173580682A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000521585.5:c.*18+15769A>G ENSP00000429863.1:n.*18+15769A>G